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  1. 1
    Punctate inner choroidopathy in common variable immunodeficiency associated with a pathogenic variant in the tumour necrosis factor receptor superfamily 13b (TNFRSF13B) gene - Case report and review of the literature

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  2. 2
    Resolving the polygenic aetiology of a late onset combined immune deficiency caused by NFKB1 haploinsufficiency and modified by PIK3R1 and TNFRSF13B variants

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  3. 3
    Fingolimod induces BAFF and expands circulating transitional B cells without activating memory B cells and plasma cells in multiple sclerosis

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  4. 4
    Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

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  5. 5
    TACI mutation in Good's Syndrome in search of a genetic basis

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  6. 6
    Lymphocyte characteristics in children with common variable immunodeficiency

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  7. 7
    High serum levels of BAFF, APRIL, and TACI in common variable immunodeficiency
    Article

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